GB1067433A - Improvements in or relating to anaerobic curing compositions - Google Patents

Improvements in or relating to anaerobic curing compositions

Info

Publication number
GB1067433A
GB1067433A GB43958/63A GB4395863A GB1067433A GB 1067433 A GB1067433 A GB 1067433A GB 43958/63 A GB43958/63 A GB 43958/63A GB 4395863 A GB4395863 A GB 4395863A GB 1067433 A GB1067433 A GB 1067433A
Authority
GB
United Kingdom
Prior art keywords
acid
butyl
hydroquinone
neopentyl glycol
acrylic
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB43958/63A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hexion UK Ltd
Original Assignee
Borden Chemical UK Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to US3125480D priority Critical patent/US3125480A/en
Application filed by Borden Chemical UK Ltd filed Critical Borden Chemical UK Ltd
Priority to GB43958/63A priority patent/GB1067433A/en
Priority to FR954963A priority patent/FR1376118A/en
Publication of GB1067433A publication Critical patent/GB1067433A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F20/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
    • C08F20/02Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
    • C08F20/10Esters
    • C08F20/20Esters of polyhydric alcohols or polyhydric phenols, e.g. 2-hydroxyethyl (meth)acrylate or glycerol mono-(meth)acrylate
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/08Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with the hydroxy or O-metal group of organic compounds
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J4/00Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 - C09J183/16

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Neopentyl glycol diacrylate and dimethacrylate are prepared by heating to boiling 1 mole of neopentyl glycol and 2.5 moles of acrylic or methacrylic acid in benzene in the presence of hydroquinone and concentrated sulphuric acid, the water of reaction being removed azeotropically and continuously. The sulphuric acid and unreacted (meth)acrylic acid are removed by washing with water.ALSO:Anaerobic curing compositions suitable for the bonding of metallic surfaces such as nuts and bolts comprise the neopentyl glycol diester of acrylic or methacrylic acid, a polymerization inhibitor, an organic peroxy compound as a polymerization initiator and, optionally, an accelerator or activator. Suitable inhibitors are hydroquinone, pyrogallol, quinhydrone and monoaryl (e.g. monophenyl) or monoalkyl (e.g. monobutyl) ethers of hydroquinone. Initiators specified are di-t.-butyl peroxide, t.-butyl hydroperoxide, t.-butyl perbenzoate, di-t.-butyl perphthalate (used in dimethyl phthalate), methyl ethyl ketone peroxide, cumene hydroperoxide and di-isopropylbenzene hydroperoxide. As accelerator there may be used benzene sulphinic acid, which may be substituted by a methyl and/or chloro group, cobalt compounds, e.g. cobalt chloride, ascorbic and isoascorbic acids, and amines such as dimethylaniline, triethanolamine and triethylamine.
GB43958/63A 1963-11-07 1963-11-07 Improvements in or relating to anaerobic curing compositions Expired GB1067433A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US3125480D US3125480A (en) 1963-11-07 Neopentyl glycol acrylate ester
GB43958/63A GB1067433A (en) 1963-11-07 1963-11-07 Improvements in or relating to anaerobic curing compositions
FR954963A FR1376118A (en) 1963-11-07 1963-11-26 Anaerobic stabilization composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB43958/63A GB1067433A (en) 1963-11-07 1963-11-07 Improvements in or relating to anaerobic curing compositions

Publications (1)

Publication Number Publication Date
GB1067433A true GB1067433A (en) 1967-05-03

Family

ID=10431124

Family Applications (1)

Application Number Title Priority Date Filing Date
GB43958/63A Expired GB1067433A (en) 1963-11-07 1963-11-07 Improvements in or relating to anaerobic curing compositions

Country Status (2)

Country Link
US (1) US3125480A (en)
GB (1) GB1067433A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2247685A (en) * 1990-09-05 1992-03-11 Johnson Matthey Plc Improvements in cross-linked polymers

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3769138A (en) * 1964-12-14 1973-10-30 D Robbiati Apparatus and a method for preparing a composite laminated sheet
US3419512A (en) * 1965-12-23 1968-12-31 Borden Inc Anaerobic curing composition
US3658624A (en) * 1969-09-29 1972-04-25 Borden Inc Bonding method employing a two part anaerobically curing adhesive composition
DE2531180C2 (en) * 1975-07-11 1982-04-01 Institut chimičeskoj fiziki Akademii Nauk SSSR, Moskva Anaerobic mixture
US4052244A (en) * 1976-08-18 1977-10-04 National Starch And Chemical Corporation Rapid curing two part adhesive
US4536267A (en) * 1983-04-01 1985-08-20 Matsushita Electric Industrial Co., Ltd. Plastic lens of neopentyl glycol dimethacrylate copolymerized with methoxy diethylene glycol methacrylate or diethylene glycol dimethacrylate

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2346644A (en) * 1940-03-18 1944-04-18 Stein Hall Mfg Co Method of bonding
US2414414A (en) * 1942-10-06 1947-01-14 Pennsylvania Coal Products Com Method of bonding materials with a cold-setting dihydroxy benzene aldehyde adhesive
FR960838A (en) * 1947-02-07 1950-04-26
BE504916A (en) * 1950-07-29 1900-01-01
DE1109891B (en) * 1955-08-25 1961-06-29 American Sealants Company Liquid mixtures that polymerize in the absence of air

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2247685A (en) * 1990-09-05 1992-03-11 Johnson Matthey Plc Improvements in cross-linked polymers

Also Published As

Publication number Publication date
US3125480A (en) 1964-03-17

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